rs1057519907

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar

Make rs1057519907(A;C)

Make rs1057519907(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

4

Position

54728057

Gene

KIT

is a	snp
is	mentioned by
dbSNP	rs1057519907
dbSNP (classic)	rs1057519907
ClinGen	rs1057519907
ebi	rs1057519907
HLI	rs1057519907
Exac	rs1057519907
Gnomad	rs1057519907
Varsome	rs1057519907
LitVar	rs1057519907
Map	rs1057519907
PheGenI	rs1057519907
Biobank	rs1057519907
1000 genomes	rs1057519907
hgdp	rs1057519907
ensembl	rs1057519907
geneview	rs1057519907
scholar	rs1057519907
google	rs1057519907
pharmgkb	rs1057519907
gwascentral	rs1057519907
openSNP	rs1057519907
23andMe	rs1057519907
SNPshot	rs1057519907
SNPdbe	rs1057519907
MSV3d	rs1057519907
GWAS Ctlg	rs1057519907

Max Magnitude

0

ClinVar
Risk	rs1057519907(C;C)
Alt	rs1057519907(C;C)
Reference	Rs1057519907(A;A)
Significance	Probable-Pathogenic
Disease	Malignant melanoma of skin Adenocarcinoma of stomach
Variation	info
Gene	KIT
CLNDBN	Malignant melanoma of skin Adenocarcinoma of stomach
Reversed	0
HGVS	NC_000004.11:g.55594223A>C
CLNSRC
CLNACC	RCV000428962.1, RCV000439220.1,